Senior Statistician

Warman O'Brien; Polska; Remote; PLN 262,000 - 437,000; Full time

Benefits offered by this job

Career progression

Learning culture

Flexible working

Competitive package

People-first culture

Job summary

Award-Winning CRO is seeking a Senior Biostatistician I or II to join their high-performing Study Delivery team. This fully remote role supports studies across UK/Europe, focusing on planning, execution, and timely delivery of high-quality statistical work.

The ideal candidate has an MS or PhD in Statistics or Biostatistics, 5+ years in a CRO/pharma biostatistics role, and strong SAS programming skills. Excellent communication and ability to translate statistics for non-technical stakeholders

Qualifications

• MS or PhD in Statistics or Biostatistics
• 5+ years' experience in biostatistics within a CRO or pharmaceutical environment
• Strong SAS programming skills and applied statistics knowledge
• Deep understanding of study designs and clinical trial methodology
• Excellent written and verbal communication; ability to explain complex stats to non-technical stakeholders

Responsibilities

• Lead biostatistics and programming activities for studies of moderate complexity
• Contribute to protocol development, design of analysis plans, and derived data
• Create tables, listings, and figures for clinical study reports
• Perform data analysis, interpret results, and write statistical methods sections
• Ensure consistency across a program of studies

Job description

Award-Winning CRO | Fully Remote | UK / Europe

Are you a seasoned Biostatistician ready to take the next step in your career with a company that values innovation, flexibility, and people-first culture? We’ve partnered with a leading, award-winning CRO that’s known for delivering excellence in clinical research and they’re looking for a Senior Biostatistician I or II to join their high-performing Study Delivery team.

As a Senior Biostatistician, you'll take the lead on biostatistics and programming activities for studies of moderate complexity - from planning and monitoring to execution and delivery. Your work will be critical to ensuring clinical trials are completed on time, within budget, and to the highest standards.

What You'll Be Doing

• Contributing to protocol development: study design, sample size calculations, and patient randomization
• Designing case report forms with statistical input
• Creating statistical analysis plans and defining derived data
• Designing and reviewing tables, listings, and figures for clinical study reports
• Performing data analysis and interpreting results
• Writing the statistical methods sections of integrated reports
• Ensuring consistency across a program of studies

Bonus: Experience in Oncology is a plus but not essential.

What We're Looking For

• M.S. or Ph.D. in Statistics, Biostatistics, or a related field
• 5+ years' experience in a biostatistics role within a CRO or pharmaceutical environment
• Strong grasp of applied parametric/nonparametric statistics and solid SAS programming skills
• In-depth knowledge of study designs and clinical trial methodology
• Strong communication skills - both written and verbal
• Ability to translate complex statistical concepts for non-technical stakeholders

This CRO isn't just another name in the industry - it's a place where careers are built, talents are nurtured, and people matter.

• Career Progression: Whether you want to grow deeper into biostatistics or explore adjacent roles, there’s a clear path forward.
• Learning Culture: You'll be empowered with coaching and mentoring opportunities, and given the space to grow your expertise.
• Flexible Working: 100% remote role with a focus on work-life balance.
• Competitive Package: Excellent salary and benefits, tailored to today’s market and your experience.
• People-First Culture: You're not just an employee - you're part of a collaborative, supportive team that feels more like family.